화학공학소재연구정보센터
Journal of Industrial and Engineering Chemistry, Vol.18, No.4, 1326-1331, July, 2012
Alkylation of phenol with tert-butyl alcohol over zirconium incorporated mesoporous molecular sieves with enhanced acidity
E-mail:
Several SO42-/Zr-MCM-41 and SO42-/Zr-MCM-48 solid acid catalysts were prepared by wet impregnation method and were characterized by FT-IR, XRD, NH3-TPD and N2 physical adsorption, respectively. The catalytic activities of these catalysts were evaluated in alkylation reaction of phenol and tert-butyl alcohol. Experimental results reveal that the four solid acid catalysts still maintained a typical mesoporous framework. Under comparable condition, the SO4 2-/Zr-MCM-48-25 catalyst exhibits much high catalytic activity and gives the highest phenol conversion as compared with the other catalysts. A maximum phenol conversion of 91.6% with 81.8% selectivity to 4-tert-butylphenol (4-TBP) was achieved at the reaction temperature of 140 ℃.
  1. Mathew T, Rao BS, Gopinath CS, J. Catal., 222(1), 107 (2004)
  2. Elavarasan P, Kondamudi K, Upadhyayula S, Chem. Eng. J., 166(1), 340 (2011)
  3. Chandler K, Deng FH, Dillow AK, Liotta CL, Eckert CA, Ind. Eng. Chem. Res., 36(12), 5175 (1997)
  4. Bhatt N, Sharma P, Patel A, Selvam P, Catal. Commun., 9, 1545 (2008)
  5. Carlton AS, J. Org. Chem., 13, 120 (1948)
  6. Chandra KG, Sharma MM, Catal. Lett., 19, 309 (1993)
  7. Shen HY, Judeh ZMA, Ching CB, Tetrahedron Lett., 44, 981 (2003)
  8. Krishnan AV, Ojha K, Pradhan NC, Org. Process Res. Dev., 6, 132 (2002)
  9. Dumitriu E, Hulea V, J. Catal., 218(2), 249 (2003)
  10. Sakthivek A, Badamali SK, Selvam P, Microporous Mesoporous Mater., 39, 457 (2000)
  11. Savidha R, Pandurangan A, Palanichamy M, Murugesan V, J. Mol. Catal. A-Chem., 211(1-2), 165 (2004)
  12. Sakthivel A, Dapurkar SE, Gupta NM, Kulshreshtha SK, Selvam P, Microporous Mesoporous Mater., 65, 177 (2003)
  13. Zhao ZK, Wang WL, Qiao WH, Wang GR, Li ZS, Cheng LB, Microporous Mesoporous Mater., 93, 164 (2006)
  14. Jiang TS, Zhao Q, Li M, Yin HB, J. Hazard. Mater., 159(2-3), 204 (2008)
  15. Clark JH, Acc. Chem. Res., 35, 791 (2002)
  16. Okuhara T, Chem. Rev., 102(10), 3641 (2002)
  17. Harmer MA, Sun Q, Appl. Catal. A: Gen., 221(1-2), 45 (2001)
  18. Anand R, Maheswari R, Gore KU, Tope BB, J. Mol. Catal. A-Chem., 193(1-2), 251 (2003)
  19. Li YX, Xue B, Yang YT, Fuel Process. Technol., 90(10), 1220 (2009)
  20. Beck JS, Vartulli JC, Roth WJ, Leonowicz ME, Kresge CT, Schmitt KD, Chu CTW, Olson DH, Sheppard EW, McCullen SB, Higgings JB, Schlenker JL, J. Am.Chem. Soc., 114, 10834 (1992)
  21. Savidha R, Pandurangan A, Palanichamy M, Murugesan V, J. Mol. Catal. A-Chem., 211(1-2), 165 (2004)
  22. Badamali SK, Sakthivel A, Selvam P, Catal. Lett., 65(1-3), 153 (2000)
  23. Parvulescu V, Su BL, Catal. Today, 69(1-4), 315 (2001)
  24. Parvulescu V, Anastasescu C, Su BL, J. Mol. Catal. A-Chem., 211(1-2), 143 (2004)
  25. Chen LF, Zhou XL, Norena LE, Wang JA, Navarrete J, Salas P, Montoya A, Del Angel P, Llanos ME, Appl. Surf. Sci., 253(5), 2443 (2006)
  26. Zhao Q, Zhou XP, Li YH, Li M, Jiang TS, Yin HB, Li CS, Appl. Surf. Sci., 255(12), 6397 (2009)
  27. Jiang TS, Wu DL, Song JN, Zhou XP, Zhao QA, Ji MR, Yin HB, Powder Technol., 207(1-3), 422 (2011)
  28. Morterra C, Cerrato G, Pinna F, Signoretto M, Strukul G, J. Catal., 149(1), 181 (1994)
  29. Li L, Yu ST, Liu FS, Yang JZ, Zhaug SF, Catal. Lett., 100(3-4), 227 (2005)
  30. Vartulli JC, Schmitt KD, Kresge CT, Roth WJ, Leonowicz ME, McCullen SB, Hellring SD, Beck JS, Schlenker JL, Olsen DH, Sheppared EW, Chem. Mater., 6, 2317 (1994)
  31. Taralkar US, Kalita P, Kumar R, Joshi PN, Appl. Catal. A: Gen., 358(1), 88 (2009)
  32. Goyvaerts D, Martens JA, Grobet PJ, Stud. Surf. Sci. Catal., 63, 381 (1991)
  33. Wu SJ, Huang JH, Wu TH, Song K, Wang HS, Xing LH, Xu HY, Xu L, Guan JQ, Kan QB, Chin. J. Catal., 27, 9 (2006)